Canonical Allele Identifier: CA1772541555

Gene: ADRA1A

Linked Data

• dbSNP Id: rs1813830727
• gnomAD v4: 8-26865355-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.26865355A>C , CM000670.2:g.26865355A>C	GRCh38
NC_000008.10:g.26722872A>C , CM000670.1:g.26722872A>C	GRCh37
NC_000008.9:g.26778789A>C	NCBI36
NG_029395.1:g.5051T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380573.4:c.-386T>G MANE Select	ENSP00000369947.3:n.-386T>G
ENST00000276393.8:c.-386T>G	ENSP00000276393.4:n.-386T>G
ENST00000380572.3:c.-386T>G	ENSP00000369946.3:n.-386T>G
ENST00000380573.3:c.-386T>G	ENSP00000369947.3:n.-386T>G
ENST00000380582.7:c.-386T>G	ENSP00000369956.3:n.-386T>G
ENST00000380586.5:c.-386T>G	ENSP00000369960.1:n.-386T>G
ENST00000519096.5:c.-386T>G	ENSP00000431073.1:n.-386T>G
ENST00000521711.5:c.-386T>G	ENSP00000430414.1:n.-386T>G
NM_000680.2:c.-386T>G	NP_000671.2:n.-386T>G
NM_033302.2:c.-386T>G	NP_150645.2:n.-386T>G
NM_033303.3:c.-386T>G	NP_150646.3:n.-386T>G
NM_033304.2:c.-386T>G	NP_150647.2:n.-386T>G
XM_005273414.3:c.-386T>G	XP_005273471.1:n.-386T>G
XM_006716292.2:c.-386T>G	XP_006716355.1:n.-386T>G
XM_006716293.2:c.-386T>G	XP_006716356.1:n.-386T>G
XM_011544411.1:c.-386T>G	XP_011542713.1:n.-386T>G
XM_011544412.1:c.-386T>G	XP_011542714.1:n.-386T>G
NM_000680.3:c.-386T>G	NP_000671.2:n.-386T>G
NM_001322502.1:c.-386T>G	NP_001309431.1:n.-386T>G
NM_001322503.1:c.-386T>G	NP_001309432.1:n.-386T>G
NM_001322504.1:c.-386T>G	NP_001309433.1:n.-386T>G
NM_033302.3:c.-386T>G	NP_150645.2:n.-386T>G
NM_033303.4:c.-386T>G	NP_150646.3:n.-386T>G
NM_033304.3:c.-386T>G	NP_150647.2:n.-386T>G
NR_136343.1:n.301T>G
XM_006716292.3:c.-386T>G	XP_006716355.1:n.-386T>G
XM_006716293.4:c.-386T>G	XP_006716356.1:n.-386T>G
XM_011544411.2:c.-386T>G	XP_011542713.1:n.-386T>G
XM_011544412.3:c.-386T>G	XP_011542714.1:n.-386T>G
XM_017013094.1:c.-386T>G	XP_016868583.1:n.-386T>G
XM_017013095.1:c.-386T>G	XP_016868584.1:n.-386T>G
XM_017013096.1:c.-386T>G	XP_016868585.1:n.-386T>G
XR_001745476.1:n.636T>G
XR_001745477.1:n.636T>G
NM_000680.4:c.-386T>G MANE Select	NP_000671.2:n.-386T>G